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Showing 3851–3860 of 18855 articles for “Art. CE 8-7-2005 n° 253291”
I.-The examination by the Agence nationale de sécurité du médicament et des produits de santé of the application for a certificate of good manufacturing practice provided for in Article R. 5131-2 of t…
…one third of the members of the Board of Directors. Unless it is an emergency, the members shall receive the agenda and the documents required to examine the subjects on the agenda at least eight day…
Service providers and equipment distributors are bound by professional secrecy. Secrecy covers not only what has been entrusted to them, but also what they have seen, read, heard, observed or understo…
The doctor responsible for medical information sends the medical board or conference and the establishment's representative the information required to analyse activity, both for the establishment as…
…n activities to combat nosocomial infections is drawn up by the operational hygiene team in accordance with a model defined by order of the Minister for Health.
…s set at national level and the indicators mentioned in article R. 6122-24. For university hospital centres, this procedure takes into account the evaluation of the commitments included in the four-ye…
A health care establishment may, in view of a particular situation, be authorised to operate an emergency facility for part of the year only, provided that the arrangements for patient care by another…
Organ transplants and haematopoietic cell transplants may not be carried out as part of the self-employed activities of statutory full-time practitioners as provided for in Article L. 6154-1.
A visit to check compliance with the safety commitments and rules is carried out by the Regional Health Agency no later than two months after the implementation of the exceptional transplant activity.…
…sed to perform organ transplants in application of article L. 1234-2 may be authorised to perform exceptional organ or tissue transplants or exceptional composite vascularised tissue transplants.
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